[骨质疏松症--新指南对实践的影响]。

Deutsche medizinische Wochenschrift (1946) Pub Date : 2024-06-01 Epub Date: 2024-05-23 DOI:10.1055/a-2127-2927
Heide Siggelkow, Friederike Thomasius
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引用次数: 0

摘要

2023 年 9 月,《绝经后女性和男性骨质疏松症的预防、诊断和治疗指南》作为全面修订的指南发布。该指南对实践的影响包括:改变了进行骨密度测量的合理指征、确定骨折风险的时间间隔、治疗阈值的水平和数量,以及针对目前存在的个体骨折风险提出的治疗方法建议。在骨质疏松症诊断中,预测脊柱和髋部骨折的风险评估至关重要。除年龄和性别外,共有 33 个风险因素可确定个人骨折风险。对跌倒风险的评估受到更多关注,并根据评估结果,结合从 65 岁开始进行肌肉训练和蛋白质摄入的建议。在确定骨质疏松症诊断指征时,还必须考虑风险指标,以及即将面临骨折风险的危险因素。基线诊断的指征已从 10 年骨折风险 >20% 变为绝经后女性和 50 岁及以上男性的诊断,具体取决于骨折风险因素情况。这就取消了基础诊断的特定骨折风险阈值。因此,在年轻患者群体(50-60 岁)中,必须考虑到医学上认为与骨质疏松症诊断指征相关的风险因素。作为开始治疗指征的新阈值是使用风险计算器确定 3 年而不是 10 年的骨折风险。药物治疗的指征应基于 DVO 风险模型的阈值。数据清楚地表明,同化疗法能够更快、更有效地降低骨折风险。在使用骨合成代谢活性物质(特立帕肽或罗莫索单抗)治疗 10%/3年以上骨折风险极高的病例中,建议首先采用这种治疗顺序。这种治疗顺序应直接启动,不应因即将进行牙科手术而推迟。为巩固降低骨折风险而进行的后续治疗应单独选择。
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[Osteoporosis - implications of the new guidelines in practice].

In September 2023, the guideline on the prophylaxis, diagnosis, and treatment of osteoporosis in postmenopausal women and men was published as a completely revised guideline. The implications for practice include a change in the justifying indication for performing a bone density measurement, the time interval over which the fracture risk is determined, the level and number of therapy thresholds, and the recommendations for the therapeutic approach that are adapted to the individual fracture risk present. Risk assessment for the prediction of spine and hip fractures is essential in the context of osteoporosis diagnostics. In addition to age and gender, there are a total of 33 risk factors to determine the individual risk of fracture. Much more attention is paid to the assessment of the risk of falls and, depending on the result, combined with recommendations for muscle training and protein intake from the age of 65. Risk indicators must also be taken into account when determining the indication for osteoporosis diagnosis, as well as the risk factors of the imminent risk of fracture. The indication for baseline diagnostics has changed from the >20% 10-year fracture risk to diagnostics in postmenopausal women and in men aged 50 years and older, depending on the fracture risk factor profile. This eliminates a specific fracture risk threshold for basic diagnostics. Thus, in the young patient group (50-60 years), the risk factors considered medically relevant for the indication for osteoporosis diagnosis must be taken into account. New thresholds as an indication for initiating therapy is the determination of fracture risk using a risk calculator over 3 years instead of 10 years. The indication for drug therapy should be based on the threshold values of the DVO risk model. The data clearly suggests a significantly faster and more effective fracture risk-reducing effect of anabolic therapy. This is recommended in the first sequence in cases of a very high risk of fracture from 10%/3 years with osteoanabolic active substances (teriparatide or romosozumab). Such a therapy sequence should be initiated directly and not delayed due to upcoming dental procedures. Follow-up therapy to consolidate the reduction of fracture risk should be chosen individually.

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